Improved Approximation Algorithms for Minimum Weight Vertex Separators

2008 ◽  
Vol 38 (2) ◽  
pp. 629-657 ◽  
Author(s):  
Uriel Feige ◽  
MohammadTaghi Hajiaghayi ◽  
James R. Lee
2019 ◽  
Vol 347 ◽  
pp. 723-733 ◽  
Author(s):  
Yingli Ran ◽  
Zhao Zhang ◽  
Xiaohui Huang ◽  
Xiaosong Li ◽  
Ding-Zhu Du

1999 ◽  
Vol 6 (39) ◽  
Author(s):  
Romeo Rizzi

<p>Let G = (V,E) be an undirected simple graph and w : E -> R+ be<br />a non-negative weighting of the edges of G. Assume V is partitioned<br />as R union X. A Steiner tree is any tree T of G such that every node<br />in R is incident with at least one edge of T. The metric Steiner tree<br />problem asks for a Steiner tree of minimum weight, given that w is a<br />metric. When X is a stable set of G, then (G,R,X) is called quasi-bipartite.<br /> In [1], Rajagopalan and Vazirani introduced the notion of<br />quasi-bipartiteness and gave a ( 3/2 + epsilon) approximation algorithm<br /> for the metric Steiner tree problem, when (G,R,X) is quasi-bipartite. In this<br />paper, we simplify and strengthen the result of Rajagopalan and Vazirani.<br />We also show how classical bit scaling techniques can be adapted<br />to the design of approximation algorithms.</p><p>Key words: Steiner tree, local search, approximation algorithm, bit scaling.</p><p> </p>


2014 ◽  
Vol 31 (2) ◽  
pp. 696-712 ◽  
Author(s):  
Dongyue Liang ◽  
Zhao Zhang ◽  
Xianliang Liu ◽  
Wei Wang ◽  
Yaolin Jiang

2016 ◽  
Vol 205 ◽  
pp. 101-108 ◽  
Author(s):  
Xiaosong Li ◽  
Zhao Zhang ◽  
Xiaohui Huang

2016 ◽  
Vol 62 (2) ◽  
pp. 441-464 ◽  
Author(s):  
Kamiel Cornelissen ◽  
Ruben Hoeksma ◽  
Bodo Manthey ◽  
N. S. Narayanaswamy ◽  
C. S. Rahul ◽  
...  

1988 ◽  
Vol 60 (02) ◽  
pp. 188-192 ◽  
Author(s):  
F A Ofosu ◽  
F Fernandez ◽  
N Anvari ◽  
C Caranobe ◽  
F Dol ◽  
...  

SummaryA recent study (Fernandez et al., Thromb. Haemostas. 1987; 57: 286-93) demonstrated that when rabbits were injected with the minimum weight of a variety of glycosaminoglycans required to inhibit tissue factor-induced thrombus formation by —80%, exogenous thrombin was inactivated —twice as fast in the post-treatment plasmas as the pre-treatment plasmas. In this study, we investigated the relationship between inhibition of thrombus formation and the extent of thrombin inhibition ex vivo. We also investigated the relationship between inhibition of thrombus formation and inhibition of prothrombin activation ex vivo. Four sulfated polysaccharides (SPS) which influence coagulation in a variety of ways were used in this study. Unfractionated heparin and the fraction of heparin with high affinity to antithrombin III potentiate the antiproteinase activity of antithrombin III. Pentosan polysulfate potentiates the activity of heparin cofactor II. At less than 10 pg/ml of plasma, all three SPS also inhibit intrinsic prothrombin activation. The fourth agent, dermatan sulfate, potentiates the activity of heparin cofactor II but fails to inhibit intrinsic prothrombin activation even at concentrations which exceed 60 pg/ml of plasma. Inhibition of thrombus formation by each sulfated polysaccharides was linearly related to the extent of thrombin inhibition achieved ex vivo. These observations confirm the utility of catalysis of thrombin inhibition as an index for assessing antithrombotic potential of glycosaminoglycans and other sulfated polysaccharides in rabbits. With the exception of pentosan polysulfate, there was no clear relationship between inhibition of thrombus formation and inhibition of prothrombin activation ex vivo.


Sign in / Sign up

Export Citation Format

Share Document